Reaktion #364584

ord-9534a44d8ccc4072bda29d1f1652439e

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled con
  2. 2
    workup.ADDITIONthe reaction mixture was poured into ice-cold water
  3. 3
    FiltrationThe yellow crystals were collected by filtration

Vorschrift

3-(4-chloro-2-fluoro-5-hydroxyphenyl)6-trifluoromethyl-2,4(1H,3H)-pyrmidinedione (2.5 g) was added to an ice cooled con. nitric acid (50 ml). After stirring for 1 hr, the reaction mixture was poured into ice-cold water. The yellow crystals were collected by filtration to afford the title compound (0.9 g). The filtrate was extracted by ethyl acetate (200 ml) and washed with brine. The organic phase was dried over anhydrous sodium sulfate. After removal of the solvent, 0.6 g of title compound was obtained as yellow crystal.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06355799B1uspto-grants-2002_03